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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156288858 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:20598274 PMID:24344687 PMID:25638461 PMID:28492532 PMID:30026338 PMID:35393742


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10406318 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:24088041 PMID:26633545


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8574770 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:24430573


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8574767 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:12075011 PMID:22504945


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8595286 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:20598274 PMID:23918765 PMID:24344687 PMID:25741868 PMID:30026338


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409144 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25638461 PMID:25741868 PMID:28492532 PMID:30026338


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13834598 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:20598274 PMID:24344687 PMID:25638461 PMID:25741868 PMID:28492532


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10403341 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:24088041 PMID:26633545 PMID:26944241 PMID:28492532 PMID:33144682


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens) & RGD:10409252|RGD:10410824|RGD:11601962|RGD:11614923|RGD:11618434|RGD:11665712|RGD:8691670|RGD:8691671|RGD:8691672|RGD:8691673|RGD:8691674 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens) & RGD:11607348|RGD:11613025|RGD:11613699|RGD:11613953|RGD:11614792|RGD:11619512|RGD:11620569|RGD:11621875|RGD:15139449 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:28492532


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens) & RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens) & RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens) & RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens) & RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens) & RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens) & RGD:11665336|RGD:11665386|RGD:11665764|RGD:11665969|RGD:126743308|RGD:152045781|RGD:404977784 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:25741868


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8574768|RGD:8574769 (Homo sapiens) & RGD:8574768|RGD:8574769 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2
  • Original References(s): PMID:24344687


    • An association has been curated linking YARS2 and myopathy, lactic acidosis, and sideroblastic anemia 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens) & RGD:11600498|RGD:11615976|RGD:11648055|RGD:11648562|RGD:11660586|RGD:11665225|RGD:11665315|RGD:11665601|RGD:11666134|RGD:11666484|RGD:28870104|RGD:28870108|RGD:28870110|RGD:28870114|RGD:28870314|RGD:28870318 (Homo sapiens)
  • 2 RGD objects have been annotated to myopathy, lactic acidosis, and sideroblastic anemia 2  (DOID:0111186)
  • 4 papers in RGD have been used to annotate YARS2
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, lactic acidosis, and sideroblastic anemia 2


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